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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

    Predicate lineage

    K121302

    Cited as predicate by: K142484, K142823, K151019, K161896, K181806, K202889, K210290

    Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.

    Manufacturer compliance record
    DateTypeOutcomeFacilityCitations
    2025-03-04VAIVoluntary action indicatedZimmer Biomet CMF and Thoracic LLC3
    2018-05-24VAIVoluntary action indicatedZimmer Biomet CMF and Thoracic LLC1
    2017-09-01VAIVoluntary action indicatedZimmer Biomet CMF and Thoracic LLC3
    2015-10-30VAIVoluntary action indicatedZimmer Biomet CMF and Thoracic LLC1
    2012-01-17VAIVoluntary action indicatedZimmer Biomet CMF and Thoracic LLC2
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